Taiwan FDA registration c52ad642ce3d9eff96062f4c755239d1

Johnson & Johnson in vitro prosthetic components (unsterilized)

TW: “強生”體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·BLATCHFORD PRODUCTS LTD.·Registered Jan 15, 2010 – Jan 15, 2025Cancelled
Registration details
Analysis ID
c52ad642ce3d9eff96062f4c755239d1
Customs Code
DHA04400846703
Company information
Manufacturer Country
United Kingdom
Authorized Representative
JOHNSON A. L. TRADING CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3420 體外肢體義肢用組件
Import Information
import
Dates and status
Registration Date
Jan 15, 2010
Expiry Date
Jan 15, 2025
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for Johnson & Johnson in vitro prosthetic components (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c52ad642ce3d9eff96062f4c755239d1 and manufactured by BLATCHFORD PRODUCTS LTD.. The authorized representative in Taiwan is JOHNSON A. L. TRADING CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including FRIDDLE "S ORTHOPEDIC APPLIANCES, PEL SUPPLY CO., and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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